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Items: 31

1.

Identifying occult maternal malignancies from 1.93 million pregnant women undergoing noninvasive prenatal screening tests.

Ji X, Li J, Huang Y, Sung PL, Yuan Y, Liu Q, Chen Y, Ju J, Zhou Y, Huang S, Chen F, Han Y, Yuan W, Fan C, Zhao Q, Wu H, Feng S, Liu W, Li Z, Chen J, Chen M, Yao H, Zeng L, Ma T, Fan S, Zhang J, Yuen KY, Cheng SH, Chik IWS, Liu NT, Zhu J, Lin S, Cao J, Tong S, Shan Z, Li W, Hekmat MR, Garshasbi M, Suela J, Torres Y, Cigudosa JC, Ruiz FJP, Rodríguez L, García M, Bernik J, Traven E, Reš U, Tul N, Tseng CF, Zhao D, Sun L, Pan Q, Shen L, Dai M, Wang Y, Wang J, Yang H, Yin Y, Duan T, Zhu B, Choolani M, Jin X, Chen Y, Mao M.

Genet Med. 2019 Apr 12. doi: 10.1038/s41436-019-0510-5. [Epub ahead of print]

PMID:
30976098
2.

Polμ deficiency induces moderate shortening of P53-/- mouse lifespan and modifies tumor spectrum.

Escudero B, Herrero D, Torres Y, Cañón S, Molina A, Carmona RM, Suela J, Blanco L, Samper E, Bernad A.

DNA Repair (Amst). 2017 Jun;54:40-45. doi: 10.1016/j.dnarep.2017.04.001. Epub 2017 Apr 10.

PMID:
28460268
3.

Recommendations for the use of microarrays in prenatal diagnosis.

Suela J, López-Expósito I, Querejeta ME, Martorell R, Cuatrecasas E, Armengol L, Antolín E, Domínguez Garrido E, Trujillo-Tiebas MJ, Rosell J, García Planells J, Cigudosa JC; Grupo de diagnóstico prenatal del INGEMM; Grupo de genética prenatal del Hospital Clínico San Carlos.

Med Clin (Barc). 2017 Apr 7;148(7):328.e1-328.e8. doi: 10.1016/j.medcli.2016.12.028. Epub 2017 Feb 21. English, Spanish.

PMID:
28233562
4.

Guidelines for genomic array analysis in acquired haematological neoplastic disorders.

Schoumans J, Suela J, Hastings R, Muehlematter D, Rack K, van den Berg E, Berna Beverloo H, Stevens-Kroef M.

Genes Chromosomes Cancer. 2016 May;55(5):480-91. doi: 10.1002/gcc.22350. Epub 2016 Feb 23.

PMID:
26774012
5.

Truncated RUNX1 protein generated by a novel t(1;21)(p32;q22) chromosomal translocation impairs the proliferation and differentiation of human hematopoietic progenitors.

Rodriguez-Perales S, Torres-Ruiz R, Suela J, Acquadro F, Martin MC, Yebra E, Ramirez JC, Alvarez S, Cigudosa JC.

Oncogene. 2016 Jan 7;35(1):125-34. doi: 10.1038/onc.2015.70. Epub 2015 Mar 23.

PMID:
25798834
6.

[Genetics applied to clinical practice in neurodevelopmental disorders].

Fernández-Jaén A, Cigudosa JC, Martín Fernández-Mayoralas D, Suela J, Fernández-Perrone AL, Calleja-Pérez B, López-Martín S.

Rev Neurol. 2014 Feb 24;58 Suppl 1:S65-70. Review. Spanish.

PMID:
25252670
7.

Microduplication 10q24.31 in a Spanish girl with scoliosis and myopathy: the critical role of LBX.

Fernández-Jaén A, Suela J, Fernández-Mayoralas DM, Fernández-Perrone AL, Wotton KR, Dietrich S, Castellanos Mdel C, Cigudosa JC, Calleja-Pérez B, López-Martín S.

Am J Med Genet A. 2014 Aug;164A(8):2074-8. doi: 10.1002/ajmg.a.36589. Epub 2014 Apr 29.

PMID:
24782348
8.

Myeloid neoplasms with der(1)t(1;19) may constitute a specific entity characterized by a cytogenetic biomarker and gene mutations involved in DNA methylation.

Salgado RN, Menezes J, Calvente M, Suela J, Acquadro F, Martínez-Laperche C, Flores R, Trujillo M, Alvarez S, Cigudosa JC.

Leuk Lymphoma. 2014 Nov;55(11):2652-5. doi: 10.3109/10428194.2014.891024. Epub 2014 Mar 17. No abstract available.

PMID:
24635575
9.

Prenatal detection of TAR syndrome in a fetus with compound inheritance of an RBM8A SNP and a 334‑kb deletion: a case report.

Papoulidis I, Oikonomidou E, Orru S, Siomou E, Kontodiou M, Eleftheriades M, Bacoulas V, Cigudosa JC, Suela J, Thomaidis L, Manolakos E.

Mol Med Rep. 2014 Jan;9(1):163-5. doi: 10.3892/mmr.2013.1788. Epub 2013 Nov 11.

PMID:
24220582
10.

Identification of prefoldin amplification (1q23.3-q24.1) in bladder cancer using comparative genomic hybridization (CGH) arrays of urinary DNA.

López V, González-Peramato P, Suela J, Serrano A, Algaba F, Cigudosa JC, Vidal A, Bellmunt J, Heredero O, Sánchez-Carbayo M.

J Transl Med. 2013 Aug 1;11:182. doi: 10.1186/1479-5876-11-182.

11.

A 2.84 Mb deletion at 21q22.11 in a patient clinically diagnosed with Marden-Walker syndrome.

Carrascosa-Romero MC, Suela J, Pardal-Fernández JM, Bermejo-Sánchez E, Vidal-Company A, MacDonald A, Tébar-Gil R, Martínez-Fernández ML, Martínez-Frías ML.

Am J Med Genet A. 2013 Sep;161A(9):2281-90. doi: 10.1002/ajmg.a.35862. Epub 2013 Jul 25.

PMID:
23894067
12.

Are ER+PR+ and ER+PR- breast tumors genetically different? A CGH array study.

Carracedo A, Salido M, Corominas JM, Rojo F, Ferreira BI, Suela J, Tusquets I, Corzo C, Segura M, Espinet B, Cigudosa JC, Arumi M, Albanell J, Serrano S, Solé F.

Cancer Genet. 2012 Apr;205(4):138-46. doi: 10.1016/j.cancergen.2012.01.001.

PMID:
22559974
13.

Neonatal detection of 5p13.2 duplication and delineation of the phenotype.

Carrascosa Romero MC, García Hoyo R, Calvente M, Baquero Cano M, González Castillo L, Suela J.

Am J Med Genet A. 2012 Apr;158A(4):877-81. doi: 10.1002/ajmg.a.35237. Epub 2012 Mar 9.

PMID:
22407779
14.

[X-chromosome-linked ichthyosis associated to epilepsy, hyperactivity, autism and mental retardation, due to the Xp22.31 microdeletion].

Carrascosa-Romero MC, Suela J, Alfaro-Ponce B, Cepillo-Boluda AJ.

Rev Neurol. 2012 Feb 16;54(4):241-8. Review. Spanish.

15.

Detection of the first gross CDC73 germline deletion in an HPT-JT syndrome family.

Cascón A, Huarte-Mendicoa CV, Javier Leandro-García L, Letón R, Suela J, Santana A, Costa MB, Comino-Méndez I, Landa I, Sánchez L, Rodríguez-Antona C, Cigudosa JC, Robledo M.

Genes Chromosomes Cancer. 2011 Nov;50(11):922-9. doi: 10.1002/gcc.20911. Epub 2011 Aug 11.

PMID:
21837707
16.

[Subtelomeric rearrangements in cryptogenic mental retardation].

Verdú Pérez A, García Murillo PL, García Campos O, López Grondona F, Arriola Pereda G, Alcaraz Rousselet MA, Vicente Lago Y, Suela J.

An Pediatr (Barc). 2011 Dec;75(6):365-71. doi: 10.1016/j.anpedi.2011.06.002. Epub 2011 Jul 27. Spanish.

17.

Primary cutaneous CD30+ anaplastic large-cell lymphomas show a heterogeneous genomic profile: an oligonucleotide arrayCGH approach.

Sánchez-Schmidt JM, Salgado R, Servitje O, Gallardo F, Ortiz-Romero PL, Karpova MB, Zipser MC, García-Muret MP, Estrach T, Rodríguez-Pinilla SM, Climent F, Suela J, Ferreira BI, Cigudosa JC, Salido M, Barranco C, Serrano S, Dummer R, Solé F, Pujol RM, Espinet B.

J Invest Dermatol. 2011 Jan;131(1):269-71. doi: 10.1038/jid.2010.271. Epub 2010 Sep 16. No abstract available.

18.

DNA methylation profiles and their relationship with cytogenetic status in adult acute myeloid leukemia.

Alvarez S, Suela J, Valencia A, Fernández A, Wunderlich M, Agirre X, Prósper F, Martín-Subero JI, Maiques A, Acquadro F, Rodriguez Perales S, Calasanz MJ, Roman-Gómez J, Siebert R, Mulloy JC, Cervera J, Sanz MA, Esteller M, Cigudosa JC.

PLoS One. 2010 Aug 16;5(8):e12197. doi: 10.1371/journal.pone.0012197.

19.

Molecular characterization of a new patient with a non-recurrent inv dup del 2q and review of the mechanisms for this rearrangement.

Vera-Carbonell A, López-Expósito I, Bafalliu JA, Ballesta-Martínez M, Glóver G, Llópis C, Moya-Quiles R, Suela J, Fernández A, Guillén-Navarro E.

Am J Med Genet A. 2010 Oct;152A(10):2670-80. doi: 10.1002/ajmg.a.33613. Review.

PMID:
20799321
20.

Deregulated expression of the polycomb-group protein SUZ12 target genes characterizes mantle cell lymphoma.

Martín-Pérez D, Sánchez E, Maestre L, Suela J, Vargiu P, Di Lisio L, Martínez N, Alves J, Piris MA, Sánchez-Beato M.

Am J Pathol. 2010 Aug;177(2):930-42. doi: 10.2353/ajpath.2010.090769. Epub 2010 Jun 17.

21.

Copy number variations are not modifiers of phenotypic expression in a pair of identical twins carrying a BRCA1 mutation.

Lasa A, Ramón y Cajal T, Llort G, Suela J, Cigudosa JC, Cornet M, Alonso C, Barnadas A, Baiget M.

Breast Cancer Res Treat. 2010 Oct;123(3):901-5. doi: 10.1007/s10549-010-0877-0. Epub 2010 Apr 6.

PMID:
20369283
22.

Oligonucleotide array-CGH identifies genomic subgroups and prognostic markers for tumor stage mycosis fungoides.

Salgado R, Servitje O, Gallardo F, Vermeer MH, Ortiz-Romero PL, Karpova MB, Zipser MC, Muniesa C, García-Muret MP, Estrach T, Salido M, Sánchez-Schmidt J, Herrera M, Romagosa V, Suela J, Ferreira BI, Cigudosa JC, Barranco C, Serrano S, Dummer R, Tensen CP, Solé F, Pujol RM, Espinet B.

J Invest Dermatol. 2010 Apr;130(4):1126-35. doi: 10.1038/jid.2009.306. Epub 2009 Sep 17.

23.

A comprehensive microarray-based DNA methylation study of 367 hematological neoplasms.

Martin-Subero JI, Ammerpohl O, Bibikova M, Wickham-Garcia E, Agirre X, Alvarez S, Brüggemann M, Bug S, Calasanz MJ, Deckert M, Dreyling M, Du MQ, Dürig J, Dyer MJ, Fan JB, Gesk S, Hansmann ML, Harder L, Hartmann S, Klapper W, Küppers R, Montesinos-Rongen M, Nagel I, Pott C, Richter J, Román-Gómez J, Seifert M, Stein H, Suela J, Trümper L, Vater I, Prosper F, Haferlach C, Cruz Cigudosa J, Siebert R.

PLoS One. 2009 Sep 11;4(9):e6986. doi: 10.1371/journal.pone.0006986.

24.

Comparative genome profiling across subtypes of low-grade B-cell lymphoma identifies type-specific and common aberrations that target genes with a role in B-cell neoplasia.

Ferreira BI, García JF, Suela J, Mollejo M, Camacho FI, Carro A, Montes S, Piris MA, Cigudosa JC.

Haematologica. 2008 May;93(5):670-9. doi: 10.3324/haematol.12221. Epub 2008 Mar 26.

25.

DNA profiling by arrayCGH in acute myeloid leukemia and myelodysplastic syndromes.

Suela J, Alvarez S, Cigudosa JC.

Cytogenet Genome Res. 2007;118(2-4):304-9. Review.

PMID:
18000384
26.

Array CGH and gene-expression profiling reveals distinct genomic instability patterns associated with DNA repair and cell-cycle checkpoint pathways in Ewing's sarcoma.

Ferreira BI, Alonso J, Carrillo J, Acquadro F, Largo C, Suela J, Teixeira MR, Cerveira N, Molares A, Goméz-López G, Pestaña A, Sastre A, Garcia-Miguel P, Cigudosa JC.

Oncogene. 2008 Mar 27;27(14):2084-90. Epub 2007 Oct 22.

PMID:
17952124
27.
28.

DNA profiling analysis of 100 consecutive de novo acute myeloid leukemia cases reveals patterns of genomic instability that affect all cytogenetic risk groups.

Suela J, Alvarez S, Cifuentes F, Largo C, Ferreira BI, Blesa D, Ardanaz M, García R, Marquez JA, Odero MD, Calasanz MJ, Cigudosa JC.

Leukemia. 2007 Jun;21(6):1224-31. Epub 2007 Mar 22.

PMID:
17377590
29.

Neurofibromatosis 1, and Not TP53, seems to be the main target of chromosome 17 deletions in de novo acute myeloid leukemia.

Suela J, Largo C, Ferreira B, Alvarez S, Robledo M, González-Neira A, Calasanz MJ, Cigudosa JC.

J Clin Oncol. 2007 Mar 20;25(9):1151-2; author reply 1152-3. No abstract available.

PMID:
17369586
30.

Expression of adhesion molecules and RANTES in kidney transplant from nonheart-beating donors.

Gomez del Moral M, Aviles B, Colberger IK, Campos-Martin Y, Suela J, Alvarez J, Perez-Contin MJ, Sánchez-Fructuoso A, Barrientos A, Martinez-Naves E.

Transpl Int. 2005 Mar;18(3):333-40.

31.

Expression of human CD1d molecules protects target cells from NK cell-mediated cytolysis.

Campos-Martín Y, Gómez del Moral M, Gozalbo-López B, Suela J, Martínez-Naves E.

J Immunol. 2004 Jun 15;172(12):7297-305.

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